Clinical Trial Management in Academic Medical Centers

Date: Wednesday, October 30
Time: 12:00pm-1:00pm PT
Audience: Audiences interested in clinical trial management.
Platform: Zoom

Clinical trials are crucial for the development of safe and effective medical products and enhancing the quality of patient care worldwide. Effective clinical trial management ensures compliance with regulatory requirements, prioritizes participant safety through safety protocols and monitoring for adverse effects, ensures research validity, as well as the collection and management of high-quality, accurate data. Above all, promoting the ethical conduct throughout the clinical trial process. This presentation introduces clinical trial management principles for academic medical center investigator sites.

Learning Objectives:

1. Introduction to clinical trial management principles.
2. Practical approaches to implementing and conducting clinical trials at academic medical centers.

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About the Speaker

Tony Succar, PhD
– MScMed(OphthSc)
– Assistant Professor
– USC Department of Regulatory and Quality Sciences, USC Mann School of Pharmacy
– 18 years clinical trials experience

Tony Succar is an Assistant Professor in the Department of Regulatory and Quality Science, USC Mann School of Pharmacy, University of Southern California. He previously worked as a Clinical Research Project Manager at Massachusetts Eye and Ear, Harvard Medical School, managing multi-center industry sponsored and investigator initiated clinical trials for drugs, biologics, medical devices and combination products. He completed his Postdoctoral Fellowship at the University of Southern California Keck School of Medicine, and earned his Master of Science in Medicine (Ophthalmic Science) and PhD from the University of Sydney.

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